const EN = {
    language: {
        set_success: 'Language was set to {language}'
    },
    theme: {
        set_success: 'Theme was set to {theme}'
    },
    menu: {
        Menu    : 'Home',
        Query   : 'QTL',
        Survival: 'Survival',
        GWAS    : 'GWAS',
        Download: 'Download',
        Help    : 'Help',
        Contact : 'Contact'
    },
    footer: {
        school         : 'HZAU',
        department     : 'College of Informatics',
        contry         : 'China',
        contact_us     : 'Contact us'
    },
    queryForm: {
        submit             : 'Submit',
        reset              : 'Reset',
        placeHolder        : 'Variant, Position or Trait',
        example            : 'e.g.',
        variant            : 'By Variant',
        trait              : 'By Trait',
        searchByVariantHelp: 'Searching by variant, you will get all the traits associating with the variant',
        searchByTraitHelp  : 'Searching by trait, you will get all the variant associating with the trait',
        allertMessages     : {
            empty       : 'Please input something',
            hasSpecial  : 'Only \'_\', \',\', and \'-\' are acceptable',
            wrongPos    : 'Invalid position',
            startWithNum: 'Cannot start with numbers'
        }

    },
    indexPage: {
        title1     : 'Pan-cancer Multi-nucleotide Variants',
        title2     : 'Molecular Quantitative Trait Locus',
        description: 'Get Started by Searching:',
        title3     : 'Get Started by Searching:',
        sample     : 'Samples',
        mnv        : 'MNVs',
        cis        : 'Cis-QTL',
        trans      : 'Trans-QTL',
        search     : 'Cis QTLs',
        survival   : 'Survival QTLs',
        gwas       : 'GWAS QTLs',
        download   : 'Data Download',
        siteinfo   : 'Multi-nucleotide variants (MNVs), defined as two or more nearby variants existing on the same haplotype in an individual, are a clinically and biologically important class of genetic variation. Pancan-MNVQTLdb integrates multi-omics resources to calculate and summarize the significant molecular features of MNVs. We get 1,322,672 cis-MNVQTLs and 321,399 trans-MNVQTLs in total. By correlating with GWAS catelog, we get 162,553 MNVQTLs relating to complex trait/disease. We also identified 67,472 survival-related MNVQTLs.'
    },
    resultPage: {
        variantCount: 'Results Found',
        cancer: 'Cancer',
        phenotype: 'Phenotype',
        variant: 'Variant',
        heatmapHeader: 'Overview of',
        tableHeader: 'Data',
        filter: 'Filter',
        rows_per_page_label: 'Records per page: '
    }
}

export default EN
